Reaction of triphenylphosphine with phenylethanethiolate-protected Au38 nanoparticles

The replacement of phenylethanethiolate (SC2Ph) ligands on 1.1 nm (core diameter) Au38(SC2Ph)24 monolayer-protected clusters (MPCs) with varied amounts of triphenylphosphine (PPh3) is investigated in methylene chloride. UV-vis spectra suggest that changes in the MPC Au core size occur when large amounts (> 10 equiv moles per cluster) of PPh3 are reacted with Au38(SC2Ph)24. 1H and 31P NMR spectra following the addition of smaller amounts (< 5 equiv moles) of PPh3 indicate that the reaction liberates a AuISC2Ph complex, as opposed to a SC2Ph thiol, disulfide, or anion. A 1H NMR kinetic study shows that the exchange is surprisingly rapid, even faster than exchanges of thiolates with other thiolates, at room temperature and in air. The reaction is slowed when cooled or conducted under Ar. The difference in potentials of the initial one-electron voltammetric reduction and oxidation of Au38(SC2Ph)24 decreases slightly upon reaction with small amounts of PPh3.     

富烯碳原子簇的石墨层间闭合形成机理

本文提出了富烯碳原子簇的石墨层间闭合形成机理，由该机理推出的许多结果与实验事实符合很好。我们认为碳原子簇自由基的快速淬灭及其淬灭速度是富烯碳原子簇形成及其丰度的决定因素。由此得出富烯碳原子簇在给定实验条件下产生的必然性，并预言不同大小的富烯碳原子簇可以通过优化实验条件选择性地合成。     

Fluorous Synthesis of Biaryl-Substituted Proline Analogs by 1,3-Dipolar Cycloaddition and Suzuki Coupling Reactions

A solution-phase synthesis of bicyclic prolines containing four points of diversity has been developed by a two-step synthesis involving 1,3-dipolar cycloaddition of perfluoroalkylsulfonyl-protected hydroxybenzaldehydes followed by Pd-catalyzed Suzuki coupling reaction of fluorous sulfonates with boronic acids. Both reactions are conducted under microwave irradiation and reaction mixtures are purified by solid-phase extractions without performing chromatography.     

Determination of mercury in human urine by neutron activation analysis,with lead diethyldithiocarbamate as a preconcentration agent

Lead diethyldithiocarbamate is an effective reagent for preconcentration of mercury in urine for neutron activation analysis. Sodium and bromine are removed from the sample by this procedure. As lead diethyldithiocarbamate is insensitive to neutron activation, radiochemical separation is not needed after neutron irradiation. Results from the analysis of urine collected from workers in caustic soda manufacturing plants are discussed.     

二芳基乙烯类光致变色材料的合成概述

由于具有多种潜在的应用价值, 光致变色化合物作为高级功能材料的研究在国内外广受关注. 在众多的有机光致变色化合物中, 二芳基乙烯特别是二噻吩乙烯, 由于其具有良好的热稳定性和优良的耐疲劳度而成为这类化合物的杰出代表. 近年来, 有关二芳基乙烯类光致变色化合物的各种合成及性能方面的报道已涉及到信息存储、分子开关、逻辑电路、液晶显示、磁性材料等众多领域. 主要是从有机合成的角度, 对这类材料的合成进行了较为全面的概括, 对各种合成方法分别加以介绍和分析, 对其发展趋势予以探索和展望.     

Determination of the atmospheric neutrino spectra with the Fréjus detector

The combined analysis of the final event set of data on neutrino interactions inside the detector, upward going stopping muons and horizontal muons recorded in the Fréjus experiment is presented. The absolute atmospheric neutrino spectra in the energy range for electron neutrinos and for muon neutrinos are determined. Based on the parameterization of Volkova for thev ^µ a spectral index of =2.66±0.05 is obtained from the ratio of horizontal muons over upward going stopping muons and from the measurement of the energy loss of horizontal muons inside the detector. The neutrino spectra are compared with various flux calculations. They do not show any evidence for neutrino oscillations in agreement with earlier analyses of the Fréjus data.Now atUniversity of Michigan, Ann Arbor, USA     

Incomplete idempotent Schröder quasigroups and related packing designs

Summary In this paper it is proved that, for any positive integern 2, 3 (mod 4),n 7, there exists an incomplete idempotent Schröder quasigroup with one hole of size two IISQ(n, 2) except forn = 10. It is also proved that for any positive integern 0, 1 (mod 4), there exists an idempotent Schröder quasigroup ISQ(n) except forn = 5 and 9. These results completely determine the spectrum of ISQ(n) and provide an application to the packing of a class of edge-coloured block designs.Research supported by NSERC grant A-5320.Research supported by NSFC grant 19231060-2.     

Electrogenerated Chemiluminescence Based on Tris(2,2′-bipyridyl) Ruthenium(II) with Hydroxyl Carboxylic Acid

Upon the electrochemical oxidation of tris(2,2′-bipyridyl) ruthenium(II) [Ru(bpy)²⁺₃] and hydroxyl carboxylic acids, for instance, citric acid, tartaric acid, malic acid, and -gluconic acid, bright electrochemiluminescences (ECLs) were observed. Different luminescent reactions were presented depending on the applied potential. The light emission was mainly caused by the reaction between alkoxide radical ion and Ru(bpy)³⁺₃below the potential +1.80 V (vs Ag/AgCl). The luminescence intensity obviously increased because of the more complex reaction process. The luminescence wavelength of 608 nm, which could be found either at higher potential than +1.80 V or in the potential range from +1.30 to +1.80 V, confirmed that ECL was caused by Ru(bpy)²⁺₃*. The factors which affect the determination and HPLC separation of the four acids were also investigated.